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Ish: Loss of Type I Collagen Telopeptide Lysyl Hydroxylation Causes Musculoskeletal Abnormalities in a Zebrafish Model of Bruck Syndrome

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6. Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen

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7. Defective collagen crosslinking in bone, but not in ligament or cartilage, in Bruck syndrome: Indications for a bone-specific telopeptide lysyl hydroxylase on chromosome 17

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8. Sarlavhasiz

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   ABIABI:AkademIndex/openalex/2026.other.036756

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    ABIABI:AkademIndex/openalex/2026.other.036757

11. Sarlavhasiz

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    ABIABI:AkademIndex/openalex/2026.other.036758

12. Sarlavhasiz

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    ABIABI:AkademIndex/openalex/2026.other.036759

13. Sarlavhasiz

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    ABIABI:AkademIndex/openalex/2026.other.036760

14. Sarlavhasiz

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    ABIABI:AkademIndex/openalex/2026.other.036761

15. Sarlavhasiz

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    ABIABI:AkademIndex/openalex/2026.other.036762

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    ABIABI:AkademIndex/openalex/2026.other.036763

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    ABIABI:AkademIndex/openalex/2026.other.036764

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    ABIABI:AkademIndex/openalex/2026.other.036765

19. Sarlavhasiz

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    ABIABI:AkademIndex/openalex/2026.other.036766

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    ABIABI:AkademIndex/openalex/2026.other.036767

21. Sarlavhasiz

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    ABIABI:AkademIndex/openalex/2026.other.036768

22. Sarlavhasiz

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    ABIABI:AkademIndex/openalex/2026.other.036769

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    ABIABI:AkademIndex/openalex/2026.other.036770

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    ABIABI:AkademIndex/openalex/2026.other.036771

25. Sarlavhasiz

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